ClinVar Miner

Submissions for variant NM_001037132.4(NRCAM):c.400T>C (p.Ser134Pro)

dbSNP: rs2153741176
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics Institute, Tel Aviv Sourasky Medical Center RCV001824184 SCV002044496 pathogenic NRCAM-related disorder 2021-12-28 no assertion criteria provided research
OMIM RCV002246517 SCV002520413 uncertain significance not provided 2022-04-25 no assertion criteria provided literature only

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